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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582226Generated: November 1, 2026

Pyridine → HCID 178427272, compound

https://huagongshe.com/reaction/1582226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 136360265HCID 136360265—
ProductHCID 178427272HCID 178427272—

Reaction Steps

A sulfur trioxide-pyridine complex (2.51 g, 15.8 mmol) was added to a solution of N-(aminoiminomethyl)-1,4-dimethyl-7-hydroxy-1H-indole-2-carboxamide methanesulfonate (1.80 g, 5.26 mmol) in pyridine (20 ml), and the resulting mixture was stirred at room temperature for 16.5 hours. The solvent was distilled off under reduced pressure and water was added to the residue. Subsequently, diethyl ether was added thereto, and the solid precipitated was collected by filtration and washed with methanol to obtain 1.43 g of 2-[[[amino(imino)methyl]amino]carbonyl]-1,4-dimethyl-1H-indol-7-yl hydrogen sulfate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734205B2
Source datasetuspto-grants-2004_05
ORD IDord-8463968602ab4c0aa0430c2cd1826371
Source noteuspto-grants-2004_05